Canonical Allele Identifier: CA374106333

Gene: FBP1

Linked Data

• gnomAD v4: 9-94605468-G-C
• MyVariant Identifiers: chr9:g.97367750G>C (hg19) ; chr9:g.94605468G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94605468G>C , CM000671.2:g.94605468G>C	GRCh38
NC_000009.11:g.97367750G>C , CM000671.1:g.97367750G>C	GRCh37
NC_000009.10:g.96407571G>C	NCBI36
NG_008174.1:g.39782C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.974C>G	ENSP00000507547.1:n.974C>G
ENST00000375326.9:c.814C>G MANE Select	ENSP00000364475.5:p.Pro272Ala
ENST00000648117.1:c.619C>G	ENSP00000498145.1:p.Pro207Ala
ENST00000375326.8:c.814C>G	ENSP00000364475.4:p.Pro272Ala
ENST00000415431.5:c.814C>G	ENSP00000408025.1:p.Pro272Ala
NM_000507.3:c.814C>G	NP_000498.2:p.Pro272Ala
NM_001127628.1:c.814C>G	NP_001121100.1:p.Pro272Ala
XM_006717005.2:c.568C>G	XP_006717068.1:p.Pro190Ala
XM_006717005.4:c.568C>G	XP_006717068.1:p.Pro190Ala
NM_000507.4:c.814C>G MANE Select	NP_000498.2:p.Pro272Ala
NM_001127628.2:c.814C>G	NP_001121100.1:p.Pro272Ala